Canonical Allele Identifier: CA476145149

Linked Data

COSMIC: COSM346331
MyVariant Identifiers: chr11:g.86663393A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952351A>G , CM000673.2:g.86952351A>G GRCh38
NC_000011.9:g.86663393A>G , CM000673.1:g.86663393A>G GRCh37
NC_000011.8:g.86341041A>G NCBI36
NG_011752.1:g.8041T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.405T>C (FZD4) MANE Select ENSP00000434034.1:p.Phe135=
ENST00000531380.1:c.405T>C (FZD4) ENSP00000434034.1:p.Phe135=
ENST00000532234.5:c.*1344A>G (PRSS23) ENSP00000436676.1:n.*1344A>G
ENST00000533902.2:c.*1066A>G (PRSS23) ENSP00000437268.1:n.*1066A>G
NM_012193.3:c.405T>C (FZD4) NP_036325.2:p.Phe135=
NR_120591.1:n.2016A>G (PRSS23)
NR_120592.1:n.1765A>G (PRSS23)
NR_120591.2:n.1714A>G (PRSS23)
NR_120592.2:n.1463A>G (PRSS23)
NM_012193.4:c.405T>C (FZD4) MANE Select NP_036325.2:p.Phe135=
NR_120591.3:n.1714A>G (PRSS23)